| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Erythrocytes, blood |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Erythrocytes [#/volume] in Blood |
| Preferred Report Name for the Observation | Erythrocytes, blood |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, improper tube, clotted specimen, hemolyzed sample, dilution of blood. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Erythrocytes [#/volume] in Blood |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 2 |
| Container Description | Lavender Top (EDTA) tube |
| Container Description | Pink Top (K2EDTA) tube |
| Container Volume | 3.0 |
| Container Volume | 3.0 |
| Container Units | milliliters |
| Container Units | milliliters |
| Specimen | Blood sample |
| Additive | Potassium/K EDTA |
| Normal Collection Volume | 3 milliliters |
| Minimum Collection Volume | 0.5 milliliters |
| Specimen Requirements | Refrigeration is required if specimen is not brought immediately to laboratory. Two blood smears should be prepared if sample is not delivered to the laboratory within 4 hrs. Sample should be analyzed within 6 hours at room temperature and 24 hrs when stored at 4 degrees C. |
| Specimen Handling Code | Critical refrigerated |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Hemoglobin (Hb) |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Hemoglobin [Mass/volume] in Blood |
| Preferred Report Name for the Observation | Hemoglobin |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | Reduced hemoglobin levels indicate anemia which is commonly caused by loss of blood, nutritional deficiency, bone marrow problems, chemotherapy, kidney failure, hyper hydration, or abnormal hemoglobin (such as that of sickle-cell disease). Increase in hemoglobin levels are due to exposure to high altitudes, smoking, dehydration, or tumors. Increase in red blood cell number or size also result in increased hemoglobin levels. Hemoglobin levels are also impacted by genetic diseases, for example porphyria. |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, improper tube, clotted specimen, hemolyzed sample, dilution of blood. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Hemoglobin [Mass/volume] in Blood |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Hematocrit |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Hematocrit [Volume Fraction] of Blood |
| Preferred Report Name for the Observation | Hematocrit |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, improper tube, clotted specimen, hemolyzed sample, dilution of blood. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Hematocrit [Volume Fraction] of Blood |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 4 |
| Container Description | Lavender Top (EDTA) tube |
| Container Description | Pink Top (K2EDTA) tube |
| Container Volume | 3.0 |
| Container Volume | 3.0 |
| Container Units | milliliters |
| Container Units | milliliters |
| Specimen | Blood sample |
| Additive | Potassium/K EDTA |
| Normal Collection Volume | 3 milliliters |
| Minimum Collection Volume | 0.5 milliliters |
| Specimen Requirements | Refrigeration is required if specimen is not brought immediately to laboratory. Two blood smears should be prepared if sample is sample is not delivered to the laboratory within 4 hrs. Sample should be analyzed within 6 hours at room temperature and 24 hrs when stored at 4 degrees C. |
| Specimen Handling Code | Critical refrigerated |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Leukocytes, blood |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Leukocytes [#/volume] in Blood |
| Preferred Report Name for the Observation | Leukocytes, blood |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, improper tube, clotted specimen, hemolyzed sample, dilution of blood. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Leukocytes [#/volume] in Blood |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 5 |
| Container Description | Lavender Top (EDTA) tube |
| Container Description | Pink Top (K2EDTA) tube |
| Container Volume | 3.0 |
| Container Volume | 3.0 |
| Container Units | milliliters |
| Container Units | milliliters |
| Specimen | Blood sample |
| Additive | Potassium/K EDTA |
| Normal Collection Volume | 3 milliliters |
| Minimum Collection Volume | 0.5 milliliters |
| Specimen Requirements | Refrigeration is required if specimen is not brought immediately to laboratory. Two blood smears should be prepared if sample is not delivered to the laboratory within 4 hrs. Sample should be analyzed within 6 hours at room temperature and 24 hrs when stored at 4 degrees C. |
| Specimen Handling Code | Critical refrigerated |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Platelets |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Platelets [#/volume] in Blood |
| Preferred Report Name for the Observation | Platelets |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, improper tube, clotted specimen, hemolyzed sample, dilution of blood. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Platelets [#/volume] in Blood |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 6 |
| Container Description | Lavender Top (EDTA) tube |
| Container Description | Pink Top (K2EDTA) tube |
| Container Volume | 3.0 |
| Container Volume | 3.0 |
| Container Units | milliliters |
| Container Units | milliliters |
| Specimen | Blood sample |
| Additive | Potassium/K EDTA |
| Normal Collection Volume | 3 milliliters |
| Minimum Collection Volume | 0.5 milliliters |
| Specimen Requirements | Refrigeration is required if specimen is not brought immediately to laboratory. Two blood smears should be prepared if sample is not delivered to the laboratory within 4 hrs. Sample should be analyzed within 6 hours at room temperature and 24 hrs when stored at 4 degrees C. |
| Specimen Handling Code | Critical refrigerated |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Mean corpuscular volume (MCV) |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Erythrocyte mean corpuscular volume [Entitic volume] |
| Preferred Report Name for the Observation | Mean corpuscular volume (MCV) |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, improper tube, clotted specimen, hemolyzed sample, dilution of blood. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Erythrocyte mean corpuscular volume [Entitic volume] |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Mean corpuscular hemoglobin (MCH) |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Erythrocyte mean corpuscular hemoglobin [Entitic mass] |
| Preferred Report Name for the Observation | Mean corpuscular hemoglobin (MCH) |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, improper tube, clotted specimen, hemolyzed sample, dilution of blood. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Erythrocyte mean corpuscular hemoglobin [Entitic mass] |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Mean corpuscular hemoglobin Concentration (MCHC) |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Erythrocyte mean corpuscular hemoglobin concentration [Mass/volume] |
| Preferred Report Name for the Observation | Mean corpuscular hemoglobin Concentration (MCHC) |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, improper tube, clotted specimen, hemolyzed sample, dilution of blood. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Erythrocyte mean corpuscular hemoglobin concentration [Mass/volume] |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Red blood cell distribution width (RDW ) |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Erythrocyte distribution width [Ratio] |
| Preferred Report Name for the Observation | Red blood cell distribution width (RDW ) |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, improper tube, clotted specimen, hemolyzed sample, dilution of blood. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Erythrocyte distribution width [Ratio] |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Basophils |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Basophils [#/volume] in Blood |
| Preferred Report Name for the Observation | Basophils |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, improper tube, clotted specimen, hemolyzed sample, dilution of blood. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Basophils [#/volume] in Blood |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | % Basophils |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Basophils/100 leukocytes in Blood |
| Preferred Report Name for the Observation | % Basophils |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, improper tube, clotted specimen, hemolyzed sample, dilution of blood. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Basophils/100 leukocytes in Blood |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Monocytes |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Monocytes [#/volume] in Blood |
| Preferred Report Name for the Observation | Monocytes |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, improper tube, clotted specimen, hemolyzed sample, dilution of blood. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Monocytes [#/volume] in Blood |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | % Monocytes |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Monocytes/100 leukocytes in Blood |
| Preferred Report Name for the Observation | % Monocytes |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, improper tube, clotted specimen, hemolyzed sample, dilution of blood. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Monocytes/100 leukocytes in Blood |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Eosinophils |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Eosinophils [#/volume] in Blood |
| Preferred Report Name for the Observation | Eosinophils |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, improper tube, clotted specimen, hemolyzed sample, dilution of blood. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Eosinophils [#/volume] in Blood |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | % Eosinophils |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Eosinophils/100 leukocytes in Blood |
| Preferred Report Name for the Observation | % Eosinophils |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, improper tube, clotted specimen, hemolyzed sample, dilution of blood. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Eosinophils/100 leukocytes in Blood |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Lymphocytes |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Lymphocytes [#/volume] in Blood |
| Preferred Report Name for the Observation | Lymphocytes |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, improper tube, clotted specimen, hemolyzed sample, dilution of blood. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Lymphocytes [#/volume] in Blood |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | % Lymphocytes |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Lymphocytes/100 leukocytes in Blood |
| Preferred Report Name for the Observation | % Lymphocytes |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, improper tube, clotted specimen, hemolyzed sample, dilution of blood. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Lymphocytes/100 leukocytes in Blood |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Neutrophils |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Neutrophils [#/volume] in Blood |
| Preferred Report Name for the Observation | Neutrophils |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, improper tube, clotted specimen, hemolyzed sample, dilution of blood. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Neutrophils [#/volume] in Blood |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | % Neutrophils |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Neutrophils/100 leukocytes in Blood |
| Preferred Report Name for the Observation | % Neutrophils |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, improper tube, clotted specimen, hemolyzed sample, dilution of blood. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Neutrophils/100 leukocytes in Blood |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Anisocytosis |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Anisocytosis [Presence] in Blood |
| Preferred Report Name for the Observation | Anisocytosis |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, improper tube, clotted specimen, hemolyzed sample, dilution of blood. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Anisocytosis [Presence] in Blood |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 21 |
| Normal Text/Codes for Categorical Observations [1] | Not detected |
| Abnormal Text/Codes for Categorical Observations [1] | detected (qualifier value) |
| Value Type | Coded Entry |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Hypochromia |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Hypochromia [Presence] in Blood |
| Preferred Report Name for the Observation | Hypochromia |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, improper tube, clotted specimen, hemolyzed sample, dilution of blood. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Hypochromia [Presence] in Blood |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 22 |
| Normal Text/Codes for Categorical Observations [1] | Not detected |
| Abnormal Text/Codes for Categorical Observations [1] | detected (qualifier value) |
| Value Type | Coded Entry |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Macrocytosis |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Macrocytes [Presence] in Blood |
| Preferred Report Name for the Observation | Macrocytosis |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, improper tube, clotted specimen, hemolyzed sample, dilution of blood. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Macrocytes [Presence] in Blood |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 23 |
| Normal Text/Codes for Categorical Observations [1] | Not detected |
| Abnormal Text/Codes for Categorical Observations [1] | detected (qualifier value) |
| Value Type | Coded Entry |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Microcytosis |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Microcytes [Presence] in Blood |
| Preferred Report Name for the Observation | Microcytosis |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, improper tube, clotted specimen, hemolyzed sample, dilution of blood. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Microcytes [Presence] in Blood |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 24 |
| Normal Text/Codes for Categorical Observations [1] | Not detected |
| Abnormal Text/Codes for Categorical Observations [1] | detected (qualifier value) |
| Value Type | Coded Entry |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Poikilocytosis |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Poikilocytosis [Presence] in Blood by Light microscopy |
| Preferred Report Name for the Observation | Poikilocytosis |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, improper tube, clotted specimen, hemolyzed sample, dilution of blood. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Poikilocytosis [Presence] in Blood by Light microscopy |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 25 |
| Normal Text/Codes for Categorical Observations [1] | Not detected |
| Abnormal Text/Codes for Categorical Observations [1] | detected (qualifier value) |
| Value Type | Coded Entry |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Polychromasia |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Polychromasia [Presence] in Blood by Light microscopy |
| Preferred Report Name for the Observation | Polychromasia |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, improper tube, clotted specimen, hemolyzed sample, dilution of blood. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Polychromasia [Presence] in Blood by Light microscopy |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 26 |
| Normal Text/Codes for Categorical Observations [1] | Not detected |
| Abnormal Text/Codes for Categorical Observations [1] | detected (qualifier value) |
| Value Type | Coded Entry |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | RBC morphology |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Erythrocyte morphology finding [Identifier] in Blood |
| Preferred Report Name for the Observation | RBC morphology |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, improper tube, clotted specimen, hemolyzed sample, dilution of blood. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Erythrocyte morphology finding [Identifier] in Blood |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 27 |
| Normal Text/Codes for Categorical Observations [1] | normal (qualifier value) |
| Abnormal Text/Codes for Categorical Observations [1] | Erythrocyte agglutination (morphologic abnormality) |
| Abnormal Text/Codes for Categorical Observations [2] | Heinz bodies (finding) |
| Abnormal Text/Codes for Categorical Observations [3] | Rouleaux (finding) |
| Abnormal Text/Codes for Categorical Observations [4] | Dimorphic red blood cell population (finding) |
| Abnormal Text/Codes for Categorical Observations [5] | Basophilic stippling, erythrocytes (finding) |
| Abnormal Text/Codes for Categorical Observations [6] | Hemoglobin C crystals (finding) |
| Abnormal Text/Codes for Categorical Observations [7] | Howell Jolly bodies (finding) |
| Abnormal Text/Codes for Categorical Observations [8] | Pappenheimer bodies (finding) |
| Abnormal Text/Codes for Categorical Observations [9] | Burr cells present (finding) |
| Abnormal Text/Codes for Categorical Observations [10] | Ringed sideroblast (finding) |
| Abnormal Text/Codes for Categorical Observations [11] | Cabot's ring bodies (finding) |
| Value Type | Coded Entry |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | WBC morphology |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Leukocyte morphology finding [Identifier] in Blood |
| Preferred Report Name for the Observation | WBC morphology |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, improper tube, clotted specimen, hemolyzed sample, dilution of blood. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Leukocyte morphology finding [Identifier] in Blood |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 28 |
| Normal Text/Codes for Categorical Observations [1] | normal (qualifier value) |
| Normal Text/Codes for Categorical Observations [2] | Segmented neutrophil (cell) |
| Normal Text/Codes for Categorical Observations [3] | Monocyte (cell) |
| Normal Text/Codes for Categorical Observations [4] | Lymphocyte (cell) |
| Abnormal Text/Codes for Categorical Observations [1] | Left shifted white blood cells (finding) |
| Abnormal Text/Codes for Categorical Observations [2] | Right shifted white blood cells (finding) |
| Abnormal Text/Codes for Categorical Observations [3] | Dohle body (finding) |
| Abnormal Text/Codes for Categorical Observations [4] | Hypersegmentation (finding) |
| Abnormal Text/Codes for Categorical Observations [5] | Ring-form neutrophil (finding) |
| Abnormal Text/Codes for Categorical Observations [6] | Pelger-Huet cell (finding) |
| Abnormal Text/Codes for Categorical Observations [7] | Drumstick nuclear appendage (finding) |
| Abnormal Text/Codes for Categorical Observations [8] | Cytoplasmic vacuolation (finding) |
| Abnormal Text/Codes for Categorical Observations [9] | Sensitized leukocyte (finding) |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Platelet morphology |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Platelet morphology finding [Identifier] in Blood |
| Preferred Report Name for the Observation | Platelet morphology |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, improper tube, clotted specimen, hemolyzed sample, dilution of blood. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Platelet morphology finding [Identifier] in Blood |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 29 |
| Normal Text/Codes for Categorical Observations [1] | normal (qualifier value) |
| Abnormal Text/Codes for Categorical Observations [1] | Platelet clumps (finding) |
| Abnormal Text/Codes for Categorical Observations [2] | Giant platelet (morphologic abnormality) |
| Abnormal Text/Codes for Categorical Observations [3] | Dysplastic platelet (morphologic abnormality) |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Color of Urine |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Color of Urine |
| Preferred Report Name for the Observation | Color of Urine |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | Dark brown or smoky urine suggests a renal source of hematuria, pink or red urine are indications of extra renal sources. Deep purple urine suggests porphyria. |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, presence of preservatives, warm sample. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Color of Urine |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 30 |
| Normal Text/Codes for Categorical Observations [1] | Normal color (finding) |
| Abnormal Text/Codes for Categorical Observations [1] | Milky urine (finding) |
| Abnormal Text/Codes for Categorical Observations [2] | Pink color (finding) |
| Abnormal Text/Codes for Categorical Observations [3] | Red color (finding) |
| Abnormal Text/Codes for Categorical Observations [4] | Dark color (finding) |
| Value Type | Coded Entry |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Clarity of Urine |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Clarity of Urine |
| Preferred Report Name for the Observation | Clarity of Urine |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | Increased turbidity of urine is an indication of increased cell numbers (erythrocytes or leukocytes), presence of bacteria, presence of crystals, lipiduria, increased mucus content, semen or fecal contamination. |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, presence of preservatives, warm sample. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Clarity of Urine |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 31 |
| Normal Text/Codes for Categorical Observations [1] | Urine: looks clear (finding) |
| Abnormal Text/Codes for Categorical Observations [1] | Cloudy urine (finding) |
| Abnormal Text/Codes for Categorical Observations [2] | Urine: turbid (finding) |
| Value Type | Coded Entry |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Erythrocytes, urine |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Erythrocytes [#/area] in Urine sediment by Automated count |
| Preferred Report Name for the Observation | Erythrocytes, urine |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | Presence of more than the occasional are an indication of hemorrhage in the urinary tract system. Dysmorphic red cells can indicate glomerulonephritis. |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, presence of preservatives, warm sample. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Erythrocytes [#/area] in Urine sediment by Automated count |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Leukocytes, urine |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Leukocytes [#/area] in Urine sediment by Automated count |
| Preferred Report Name for the Observation | Leukocytes, urine |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | Presence of more than the occasional leukocytes are an indication of inflammation in the genitourinary tract. |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, presence of preservatives, warm sample. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Leukocytes [#/area] in Urine sediment by Automated count |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Leukocyte clumps, urine |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Leukocyte clumps [#/area] in Urine sediment by Automated count |
| Preferred Report Name for the Observation | Leukocyte clumps, urine |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | Clumping leukocytes occur with a high number of leukocytes, a good indicator of inflammation in the genitourinary tract. |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, presence of preservatives, warm sample. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Leukocyte clumps [#/area] in Urine sediment by Automated count |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Non-squamous epithelial cells. , urine |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Epithelial cells.non-squamous [#/area] in Urine sediment by Automated count |
| Preferred Report Name for the Observation | Non-squamous epithelial cells, urine |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | Any large number of non-squamous epithelial cells can indicate a neoplasm in the genitourinary tract. A follow up cytological analysis is recommended, when neoplasia is suspected. |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, presence of preservatives, warm sample. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Epithelial cells.non-squamous [#/area] in Urine sediment by Automated count |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Squamous epithelial cells. , urine |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Epithelial cells.squamous [#/area] in Urine sediment by Automated count |
| Preferred Report Name for the Observation | Squamous epithelial cells. , urine |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | A few squamous epithelial cells are normal in random urine, a large number suggests contamination of the sample, by incorrectly or insufficiently cleaning prior to collection. |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, presence of preservatives, warm sample. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Epithelial cells.squamous [#/area] in Urine sediment by Automated count |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Bacteria, urine |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Bacteria [#/area] in Urine sediment by Automated count |
| Preferred Report Name for the Observation | Bacteria, urine |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | Presence of bacteria, especially in large numbers indicate infection in the urinary tract. A urine culture is recommended. |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, presence of preservatives, warm sample. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Bacteria [#/area] in Urine sediment by Automated count |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Crystals , urine |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Crystals [#/area] in Urine sediment by Automated count |
| Preferred Report Name for the Observation | Crystals , urine |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This is most useful in warm fresh urine for differential diagnosis of hematuria, nephrolithiasis or toxin ingestion. There are several types of crystals indicating different disease origin. Review of urine pH as well as the polarizing microscopy are recommended for further identification. |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, presence of preservatives, warm sample. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Crystals [#/area] in Urine sediment by Automated count |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Hyaline casts |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Hyaline casts [#/area] in Urine sediment by Automated count |
| Preferred Report Name for the Observation | Hyaline casts |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | Hyaline casts are the most common type of casts. They are solidified Tamm-Horsfall mucoprotein secreted from the tubular epithelial cells of individual nephrons. Low urine flow, concentrated urine, or an acidic environment can contribute to the formation of hyaline casts, and, as such, they may be seen in normal individuals in dehydration or vigorous exercise. They often form the basis of other cast types due to inclusion or adhesion of other elements and can also indicate several types of renal disease. |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, presence of preservatives, warm sample. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Hyaline casts [#/area] in Urine sediment by Automated count |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Casts |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Casts [#/area] in Urine sediment by Automated count |
| Preferred Report Name for the Observation | Casts |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | Any kind of casts are counted in this test - there are several kinds of casts: Granular casts are the second-most common type of cast, resulting from break down of cellular casts, or inclusion of plasma proteins. They are most often indicative of chronic renal disease. Exception here is the muddy brown cast, which is an indication of acute tubular necrosis. Waxy casts can be found in urine from patients in renal failure. Fatty casts are indictors of high protein nephrotic syndrome. Pigment casts can indicate hemolytic anemia, rhobdomyolysis and liver disease. They also occur with some medication. Cellular casts: Red blood cell cast always indicate glomerular damage. White blood cell casts are suggestive of pyelonephritis, and may also be seen in inflammatory states, such as acute allergic interstitial nephritis, nephrotic syndrome, or post-streptococcal acute glomerulonephritis. |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, presence of preservatives, warm sample. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Casts [#/area] in Urine sediment by Automated count |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Spermatozoa, urine |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Spermatozoa [#/area] in Urine sediment by Automated count |
| Preferred Report Name for the Observation | Spermatozoa, urine |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | Presence of sperm in male urine can be indicative of retrograde ejaculation. |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, presence of preservatives, warm sample. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Spermatozoa [#/area] in Urine sediment by Automated count |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Mucus, urine |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Mucus [#/area] in Urine sediment by Automated count |
| Preferred Report Name for the Observation | mucus, urine |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | In the majority presence of mucus in urine is an indicator of a urinary tract infection. Other causes are kidney stone or neoplasm. |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, presence of preservatives, warm sample. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Mucus [#/area] in Urine sediment by Automated count |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Total bilirubin, urine |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Bilirubin.total [Mass/volume] in Urine by Automated test strip |
| Preferred Report Name for the Observation | Total bilirubin, urine |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | Bilirubin in urine may indicate liver damage or disease. |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, presence of preservatives, warm sample. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Bilirubin.total [Mass/volume] in Urine by Automated test strip |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 43 |
| Normal Text/Codes for Categorical Observations [1] | Not detected |
| Abnormal Text/Codes for Categorical Observations [1] | Present + out of ++++ (qualifier value) |
| Abnormal Text/Codes for Categorical Observations [2] | Present ++ out of ++++ (qualifier value) |
| Abnormal Text/Codes for Categorical Observations [3] | Present +++ out of ++++ (qualifier value) |
| Abnormal Text/Codes for Categorical Observations [4] | Present ++++ out of ++++ (qualifier value) |
| Value Type | Coded Entry |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Glucose, urine |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Glucose [Presence] in Urine |
| Preferred Long Name for the Observation | Glucose, Semi quantitative, Urine |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | Test for detection and monitoring of diabetes mellitus. |
| Patient Preparation | Collect random urine in a clean plastic container. Label the urine container with the patient's full name and the date and time of collection, refrigerate after collection. |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, presence of preservatives, warm sample. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Glucose [Presence] in Urine |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 44 |
| Container Description | Sterile, plastic, leak proof container |
| Container Volume | 4 |
| Container Units | fluid ounce (US) |
| Specimen | Urine specimen |
| Normal Collection Volume | 20 milliliter |
| Minimum Collection Volume | 4 milliliter |
| Specimen Requirements | Keep refrigerated |
| Specimen Handling Code | Refrigerated temperature |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Hemoglobin, urine |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Hemoglobin [Mass/volume] in Urine by Automated test strip |
| Preferred Report Name for the Observation | Hemoglobin, urine |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | Presence of hemoglobin is often associated with hemolytic or sickle cell anemia, though it requires work up for renal cancer, pyelonephritis, tuberculosis or malaria, and acute lead poisoning and trauma. In small amounts it may occur after strenuous exercise. |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, presence of preservatives, warm sample. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Hemoglobin [Mass/volume] in Urine by Automated test strip |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 45 |
| Normal Text/Codes for Categorical Observations [1] | Not detected |
| Abnormal Text/Codes for Categorical Observations [1] | Present + out of ++++ (qualifier value) |
| Abnormal Text/Codes for Categorical Observations [2] | Present ++ out of ++++ (qualifier value) |
| Abnormal Text/Codes for Categorical Observations [3] | Present +++ out of ++++ (qualifier value) |
| Abnormal Text/Codes for Categorical Observations [4] | Present ++++ out of ++++ (qualifier value) |
| Value Type | Coded Entry |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 45 |
| Container Description | Sterile, plastic, leak proof container |
| Container Volume | 4 |
| Container Units | fluid ounce (US) |
| Specimen | Urine specimen |
| Normal Collection Volume | 20 milliliter |
| Minimum Collection Volume | 4 milliliter |
| Specimen Requirements | Keep refrigerated |
| Specimen Handling Code | Refrigerated temperature |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Ketones , urine |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Ketones [Mass/volume] in Urine by Automated test strip |
| Preferred Report Name for the Observation | Ketones , urine |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | Ketones in urine occur more commonly in type I diabetes mellitus, but can also be observed during starvation. |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, presence of preservatives, warm sample. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Ketones [Mass/volume] in Urine by Automated test strip |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 46 |
| Normal Text/Codes for Categorical Observations [1] | Not detected |
| Abnormal Text/Codes for Categorical Observations [1] | Present + out of ++++ (qualifier value) |
| Abnormal Text/Codes for Categorical Observations [2] | Present ++ out of ++++ (qualifier value) |
| Abnormal Text/Codes for Categorical Observations [3] | Present +++ out of ++++ (qualifier value) |
| Abnormal Text/Codes for Categorical Observations [4] | Present ++++ out of ++++ (qualifier value) |
| Value Type | Coded Entry |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Leukocyte esterase, urine |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Leukocyte esterase [Presence] in Urine by Automated test strip |
| Preferred Report Name for the Observation | Leukocyte esterase, urine |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | Presence of leukocyte esterase can be used as a screening for urinary tract infection, though even in combination with nitrite results the sensitivity (24%) and specificity (94%) are low. A urine culture is the gold standard diagnosing a urinary tract infection and is recommended. |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, presence of preservatives, warm sample. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Leukocyte esterase [Presence] in Urine by Automated test strip |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 47 |
| Normal Text/Codes for Categorical Observations [1] | Not detected |
| Abnormal Text/Codes for Categorical Observations [1] | Present + out of ++++ (qualifier value) |
| Abnormal Text/Codes for Categorical Observations [2] | Present ++ out of ++++ (qualifier value) |
| Abnormal Text/Codes for Categorical Observations [3] | Present +++ out of ++++ (qualifier value) |
| Abnormal Text/Codes for Categorical Observations [4] | Present ++++ out of ++++ (qualifier value) |
| Value Type | Coded Entry |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Nitrite, urine |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Nitrite [Presence] in Urine by Automated test strip |
| Preferred Report Name for the Observation | Nitrite, urine |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This test is often included as a screening test for urinary tract infections, however it has been found to have low sensitivity (24%) and specificity (94%), even when used in combination with results from the Leukocyte Esterase test. The best test for urinary tract infect detection is still the urine culture. |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, presence of preservatives, warm sample. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Nitrite [Presence] in Urine by Automated test strip |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 48 |
| Normal Text/Codes for Categorical Observations [1] | Not detected |
| Abnormal Text/Codes for Categorical Observations [1] | Present + out of ++++ (qualifier value) |
| Abnormal Text/Codes for Categorical Observations [2] | Present ++ out of ++++ (qualifier value) |
| Abnormal Text/Codes for Categorical Observations [3] | Present +++ out of ++++ (qualifier value) |
| Abnormal Text/Codes for Categorical Observations [4] | Present ++++ out of ++++ (qualifier value) |
| Value Type | Coded Entry |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 48 |
| Container Description | Sterile, plastic, leak proof container |
| Container Volume | 4 |
| Container Units | fluid ounce (US) |
| Specimen | Urine specimen |
| Normal Collection Volume | 20 milliliter |
| Minimum Collection Volume | 4 milliliter |
| Specimen Requirements | Keep refrigerated |
| Specimen Handling Code | Refrigerated temperature |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Urine pH |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | pH of Urine by Automated test strip |
| Preferred Report Name for the Observation | Urine pH |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | Changes in pH are an indicator of the acid-base balance in the body, which may be helpful in determining subtle presence of distal renal tubular disease or pyelonephritis as well as identifying crystals in urine and determining predisposition to form a given type of stone. |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, presence of preservatives, warm sample. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | pH of Urine by Automated test strip |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 49 |
| Container Description | Sterile, plastic, leak proof container |
| Container Volume | 4 |
| Container Units | fluid ounce (US) |
| Specimen | Urine specimen |
| Normal Collection Volume | 20 milliliter |
| Minimum Collection Volume | 4 milliliter |
| Specimen Requirements | Keep refrigerated |
| Specimen Handling Code | Refrigerated temperature |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Protein, urine |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Protein [Mass/volume] in Urine by Automated test strip |
| Preferred Report Name for the Observation | Protein, urine |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | Proteinuria is an indication of kidney disease, which can be caused by several conditions, most commonly diabetes mellitus and hypertension. Other cause of protein in urine are toxins, some medications, trauma or infections. Proteinuria can also occur in pregnant women as part of preeclampsia. |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, presence of preservatives, warm sample. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Protein [Mass/volume] in Urine by Automated test strip |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 50 |
| Container Description | Sterile, plastic, leak proof container |
| Container Volume | 4 |
| Container Units | fluid ounce (US) |
| Specimen | Urine specimen |
| Normal Collection Volume | 20 milliliter |
| Minimum Collection Volume | 4 milliliter |
| Specimen Requirements | Keep refrigerated |
| Specimen Handling Code | Refrigerated temperature |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Urobilinogen |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Urobilinogen [Mass/volume] in Urine by Automated test strip |
| Preferred Report Name for the Observation | Urobilinogen |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | Urinary urobilinogen may be increased in the presence of a hemolytic process such as hemolytic anemia. It may also be increased with infectious hepatitis, or with cirrhosis. |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, presence of preservatives, warm sample. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Urobilinogen [Mass/volume] in Urine by Automated test strip |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 51 |
| Container Description | Sterile, plastic, leak proof container |
| Container Volume | 4 |
| Container Units | fluid ounce (US) |
| Specimen | Urine specimen |
| Normal Collection Volume | 20 milliliter |
| Minimum Collection Volume | 4 milliliter |
| Specimen Requirements | Keep refrigerated |
| Specimen Handling Code | Refrigerated temperature |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Urine specific gravity |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Specific gravity of Urine by Automated test strip |
| Preferred Report Name for the Observation | Urine specific gravity |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | The specific gravity of urine is used to obtain information about the state of the kidney and the state of hydration of the patient. |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling, presence of preservatives, warm sample. |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Specific gravity of Urine by Automated test strip |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 52 |
| Container Description | Sterile, plastic, leak proof container |
| Container Volume | 4 |
| Container Units | fluid ounce (US) |
| Specimen | Urine specimen |
| Normal Collection Volume | 20 milliliter |
| Minimum Collection Volume | 4 milliliter |
| Specimen Requirements | Keep refrigerated |
| Specimen Handling Code | Refrigerated temperature |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Serum Glucose |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Glucose [Mass/volume] in Serum or Plasma |
| Preferred Report Name for the Observation | Serum Glucose |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Glucose [Mass/volume] in Serum or Plasma |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 53 |
| Container Description | Gold Serum Separator tube |
| Container Description | Red, No Additive tube |
| Container Volume | 5.0 |
| Container Volume | 5.0 |
| Container Units | mililiter |
| Container Units | mililiter |
| Specimen | Serum specimen |
| Normal Collection Volume | 1 milliliter |
| Minimum Collection Volume | 0.5 milliliter |
| Specimen Requirements | Protect from light. Allow serum tube to clot completely at room temperature. Separate serum or plasma from cells ASAP or within 30 minutes of collection. |
| Specimen Handling Code | Refrigerated temperature |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Blood Urea Nitrogen (BUN) |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Urea nitrogen [Mass/volume] in Serum or Plasma |
| Preferred Report Name for the Observation | Blood Urea Nitrogen (BUN) |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Urea nitrogen [Mass/volume] in Serum or Plasma |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 54 |
| Container Description | Gold Serum Separator tube |
| Container Description | Red, No Additive tube |
| Container Volume | 5.0 |
| Container Volume | 5.0 |
| Container Units | mililiter |
| Container Units | mililiter |
| Specimen | Serum specimen |
| Normal Collection Volume | 1 milliliter |
| Minimum Collection Volume | 0.5 milliliter |
| Specimen Requirements | Protect from light. Allow serum tube to clot completely at room temperature. Separate serum or plasma from cells ASAP or within 30 minutes of collection. |
| Specimen Handling Code | Refrigerated temperature |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Creatinine |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Creatinine [Mass/volume] in Serum or Plasma |
| Preferred Report Name for the Observation | Creatinine |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Creatinine [Mass/volume] in Serum or Plasma |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 55 |
| Container Description | Gold Serum Separator tube |
| Container Description | Red, No Additive tube |
| Container Volume | 5.0 |
| Container Volume | 5.0 |
| Container Units | mililiter |
| Container Units | mililiter |
| Specimen | Serum specimen |
| Normal Collection Volume | 1 milliliter |
| Minimum Collection Volume | 0.5 milliliter |
| Specimen Requirements | Protect from light. Allow serum tube to clot completely at room temperature. Separate serum or plasma from cells ASAP or within 30 minutes of collection. |
| Specimen Handling Code | Refrigerated temperature |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | BUN/Creatinine Ratio |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Urea nitrogen/Creatinine [Mass Ratio] in Serum or Plasma |
| Preferred Report Name for the Observation | BUN/Creatinine Ratio |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Urea nitrogen/Creatinine [Mass Ratio] in Serum or Plasma |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | GFR, calculated |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Glomerular filtration rate/1.73 sq M.predicted by Creatinine-based formula (MDRD) |
| Preferred Report Name for the Observation | GFR, calculated |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Glomerular filtration rate/1.73 sq M.predicted by Creatinine-based formula (MDRD) |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Calcium |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Calcium [Mass/volume] in Serum or Plasma |
| Preferred Report Name for the Observation | Calcium |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Calcium [Mass/volume] in Serum or Plasma |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 58 |
| Container Description | Gold Serum Separator tube |
| Container Description | Red, No Additive tube |
| Container Volume | 5.0 |
| Container Volume | 5.0 |
| Container Units | mililiter |
| Container Units | mililiter |
| Specimen | Serum specimen |
| Normal Collection Volume | 1 milliliter |
| Minimum Collection Volume | 0.5 milliliter |
| Specimen Requirements | Protect from light. Allow serum tube to clot completely at room temperature. Separate serum or plasma from cells ASAP or within 30 minutes of collection. |
| Specimen Handling Code | Refrigerated temperature |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Total protein, serum |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Protein [Mass/volume] in Serum or Plasma |
| Preferred Report Name for the Observation | Total protein, serum |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Protein [Mass/volume] in Serum or Plasma |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 59 |
| Container Description | Gold Serum Separator tube |
| Container Description | Red, No Additive tube |
| Container Volume | 5.0 |
| Container Volume | 5.0 |
| Container Units | mililiter |
| Container Units | mililiter |
| Specimen | Serum specimen |
| Normal Collection Volume | 1 milliliter |
| Minimum Collection Volume | 0.5 milliliter |
| Specimen Requirements | Protect from light. Allow serum tube to clot completely at room temperature. Separate serum or plasma from cells ASAP or within 30 minutes of collection. |
| Specimen Handling Code | Refrigerated temperature |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Albumin |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Albumin [Mass/volume] in Serum or Plasma |
| Preferred Report Name for the Observation | Albumin |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Albumin [Mass/volume] in Serum or Plasma |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 60 |
| Container Description | Gold Serum Separator tube |
| Container Description | Red, No Additive tube |
| Container Volume | 5.0 |
| Container Volume | 5.0 |
| Container Units | mililiter |
| Container Units | mililiter |
| Specimen | Serum specimen |
| Normal Collection Volume | 1 milliliter |
| Minimum Collection Volume | 0.5 milliliter |
| Specimen Requirements | Protect from light. Allow serum tube to clot completely at room temperature. Separate serum or plasma from cells ASAP or within 30 minutes of collection. |
| Specimen Handling Code | Refrigerated temperature |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Globulin |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Globulin [Mass/volume] in Serum by calculation |
| Preferred Report Name for the Observation | Globulin |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Globulin [Mass/volume] in Serum by calculation |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Albumin/globulin ratio |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Albumin/Globulin [Mass Ratio] in Serum or Plasma |
| Preferred Report Name for the Observation | Albumin/globulin ratio |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Albumin/Globulin [Mass Ratio] in Serum or Plasma |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Total bilirubin, serum |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Bilirubin.total [Mass/volume] in Serum or Plasma |
| Preferred Report Name for the Observation | Total bilirubin, serum |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Bilirubin.total [Mass/volume] in Serum or Plasma |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 63 |
| Container Description | Gold Serum Separator tube |
| Container Description | Red, No Additive tube |
| Container Volume | 5.0 |
| Container Volume | 5.0 |
| Container Units | mililiter |
| Container Units | mililiter |
| Specimen | Serum specimen |
| Normal Collection Volume | 1 milliliter |
| Minimum Collection Volume | 0.5 milliliter |
| Specimen Requirements | Protect from light. Allow serum tube to clot completely at room temperature. Separate serum or plasma from cells ASAP or within 30 minutes of collection. |
| Specimen Handling Code | Refrigerated temperature |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Alkaline phosphatase (ALP) |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Alkaline phosphatase [Enzymatic activity/volume] in Serum or Plasma |
| Preferred Report Name for the Observation | Alkaline phosphatase (ALP) |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Alkaline phosphatase [Enzymatic activity/volume] in Serum or Plasma |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 64 |
| Container Description | Gold Serum Separator tube |
| Container Description | Red, No Additive tube |
| Container Volume | 5.0 |
| Container Volume | 5.0 |
| Container Units | mililiter |
| Container Units | mililiter |
| Specimen | Serum specimen |
| Normal Collection Volume | 1 milliliter |
| Minimum Collection Volume | 0.5 milliliter |
| Specimen Requirements | Protect from light. Allow serum tube to clot completely at room temperature. Separate serum or plasma from cells ASAP or within 30 minutes of collection. |
| Specimen Handling Code | Refrigerated temperature |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Alanine aminotransferase (ALT) |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Alanine aminotransferase [Enzymatic activity/volume] in Serum or Plasma |
| Preferred Report Name for the Observation | Alanine aminotransferase (ALT) |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Alanine aminotransferase [Enzymatic activity/volume] in Serum or Plasma |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 65 |
| Container Description | Gold Serum Separator tube |
| Container Description | Red, No Additive tube |
| Container Volume | 5.0 |
| Container Volume | 5.0 |
| Container Units | mililiter |
| Container Units | mililiter |
| Specimen | Serum specimen |
| Normal Collection Volume | 1 milliliter |
| Minimum Collection Volume | 0.5 milliliter |
| Specimen Requirements | Protect from light. Allow serum tube to clot completely at room temperature. Separate serum or plasma from cells ASAP or within 30 minutes of collection. |
| Specimen Handling Code | Refrigerated temperature |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Aspartate aminotransferase (ASP) |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Aspartate aminotransferase [Enzymatic activity/volume] in Serum or Plasma |
| Preferred Report Name for the Observation | Aspartate aminotransferase (ASP) |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Aspartate aminotransferase [Enzymatic activity/volume] in Serum or Plasma |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 66 |
| Container Description | Gold Serum Separator tube |
| Container Description | Red, No Additive tube |
| Container Volume | 5.0 |
| Container Volume | 5.0 |
| Container Units | mililiter |
| Container Units | mililiter |
| Specimen | Serum specimen |
| Normal Collection Volume | 1 milliliter |
| Minimum Collection Volume | 0.5 milliliter |
| Specimen Requirements | Protect from light. Allow serum tube to clot completely at room temperature. Separate serum or plasma from cells ASAP or within 30 minutes of collection. |
| Specimen Handling Code | Refrigerated temperature |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Sodium, serum |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Sodium [Moles/volume] in Serum or Plasma |
| Preferred Report Name for the Observation | Sodium, serum |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Sodium [Moles/volume] in Serum or Plasma |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Potassium, serum |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Potassium [Moles/volume] in Serum or Plasma |
| Preferred Report Name for the Observation | Potassium, serum |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Potassium [Moles/volume] in Serum or Plasma |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Chloride, serum |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Chloride [Moles/volume] in Serum or Plasma |
| Preferred Report Name for the Observation | Chloride, serum |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Chloride [Moles/volume] in Serum or Plasma |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Carbon dioxide, serum |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Carbon dioxide, total [Moles/volume] in Serum or Plasma |
| Preferred Report Name for the Observation | Carbon dioxide, serum |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Carbon dioxide, total [Moles/volume] in Serum or Plasma |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Anion gap |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Anion gap in Serum or Plasma |
| Preferred Report Name for the Observation | Anion gap |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Anion gap in Serum or Plasma |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Gamma-Glutamyltransferase (GGT) |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Gamma glutamyl transferase [Enzymatic activity/volume] in Serum or Plasma |
| Preferred Report Name for the Observation | Gamma-Glutamyltransferase (GGT) |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Interpretation of Observations | This blood test is used to determine... |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Gamma glutamyl transferase [Enzymatic activity/volume] in Serum or Plasma |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Prostate Biopsy Pathology Report |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Prostate Pathology biopsy report |
| Preferred Report Name for the Observation | Prostate Biopsy Pathology Report |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Outside Site(s) Where Observation may be Performed | Pacific Anatomic Pathology Services |
| Outside Site(s) Where Observation may be Performed | Acme Laboratories - Los Angeles |
| Address of Outside Site(s) | 2216 Santa Monica Blvd
Santa Monica CA 90404 USA |
| Address of Outside Site(s) | 8635 West 3rd Street
Los Angeles CA 90048 USA |
| Interpretation of Observations | Histologic evaluation of prostate biopsy specimens and additional prognostic information following histologic diagnosis. These tests help clinicians to diagnose prostate cancer. |
| Contraindications to Observations | Contraindications to prostate biopsy include acute painful perianal disorders, bleeding diathesis, acute prostatitis, and severe immunosuppression. |
| Contraindications to Observations | Acute prostatitis |
| Factors that may Affect the Observation | Specimen submitted unfixed; improperly labeled specimen; unlabeled specimen |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Outside Lab |
| Prior Resuts Instructions | When ordering a Prostate biopsy, send prior Prostate Specific Antigen (PSA) results |
| Prior Resuts Instructions | When ordering a Prostate biopsy, send prior relevant clinical findings. |
| Special Instructions | Submit Surgical Pathology Requisition and Biopsy Worksheet with specimen |
| Observation Identifier | Prostate Pathology biopsy report |
| Expected Turn-Around Time | 3 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 73 |
| Normal Text/Codes for Categorical Observations [1] | normal (qualifier value) |
| Abnormal Text/Codes for Categorical Observations [1] | Gleason Score 2-4: Well differentiated (finding) |
| Abnormal Text/Codes for Categorical Observations [2] | Gleason Score 5-6: Moderately differentiated (finding) |
| Abnormal Text/Codes for Categorical Observations [3] | Gleason Score 7-10: Poorly differentiated (finding) |
| Abnormal Text/Codes for Categorical Observations [4] | Atypical proliferation (morphologic abnormality) |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 73 |
| Container Description | 15 ml jar containing OncoFix II |
| Specimen | Prostate biopsy sample |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | TSH |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Thyrotropin [Units/volume] in Serum or Plasma |
| Preferred Report Name for the Observation | TSH - Serum |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Factors that may Affect the Observation | Medicines that may affect test results include: Amiodarone Dopamine Lithium Potassium iodide Prednisone |
| Service/Test/Observation Performance Schedule | Daily |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Thyrotropin [Units/volume] in Serum or Plasma |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 74 |
| Container Description | Lavender Top (EDTA) tube |
| Container Description | Pink Top (K2EDTA) tube |
| Container Volume | 3.0 |
| Container Volume | 3.0 |
| Container Units | milliliters |
| Container Units | milliliters |
| Specimen | Blood sample |
| Additive | Potassium/K EDTA |
| Normal Collection Volume | 3 milliliters |
| Minimum Collection Volume | 0.5 milliliters |
| Specimen Requirements | Refrigeration is required if specimen is not brought immediately to laboratory. Two blood smears should be prepared if sample is not delivered to the laboratory within 4 hrs. Sample should be analyzed within 6 hours at room temperature and 24 hrs when stored at 4 degrees C. |
| Specimen Handling Code | Critical refrigerated |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Pap Test |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Cytology report of Cervical or vaginal smear or scraping Cyto stain.thin prep |
| Preferred Report Name for the Observation | Pap Test |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Outside Site(s) Where Observation may be Performed | Pacific Anatomic Pathology Services |
| Address of Outside Site(s) | 2216 Santa Monica Blvd
Santa Monica CA 90404 USA |
| Observations Required to Interpret the Observation | Did the patient have a previous abnormal Pap report, treatment, or biopsy? |
| Observations Required to Interpret the Observation | Date last menstrual period |
| Interpretation of Observations | The Pap Test is for use in screening for the presence of atypical cells, cervical cancer, or precursor lesions (LSIL, HSIL) as well as other cytologic categories as defined by the Bethesda System for Reporting Cervical Cytology. |
| Patient Preparation | Instruct the patient not to douche or engage in sexual intercourse within 24 hours of the procedure. For premenopausal patients, obtain specimens during the second half of the menstrual period to avoid contamination by obscuring blood. |
| Factors that may Affect the Observation | Frozen specimens, Specimens not collected in a ThinPrep Pap Test collection kit or specimens submitted in an expired collection kit. |
| Service/Test/Observation Performance Schedule | Mon-Fri |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Other Names | ThinPrep Pap Test |
| Other Names | Pap Smear |
| Observation Identifier | 47527-7 LN |
| Expected Turn-Around Time | 2 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 75 |
| Normal Text/Codes for Categorical Observations [1] | Negative for intraepithelial lesion or malignancy |
| Value Type | Coded Entry |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 75 |
| Container Description | PreservCyt Solution vial |
| Specimen | Endocervical cytologic material |
| Additive | PreservCyt Solution |
| Specimen Requirements | Follow instructions per the ThinPrep Pap Test collection kit. |
| Specimen Handling Code | Ambient temperature |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Hepatitis A IgM antibodies (IgM anti-HAV) |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Hepatitis A virus IgM Ab [Presence] in Serum |
| Preferred Short Name or Mnemonic for Observation | IgM anti-HAV |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Observation Identifier | Hepatitis A virus IgM Ab [Presence] in Serum |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 76 |
| Normal Text/Codes for Categorical Observations [1] | Negative (qualifier value) |
| Abnormal Text/Codes for Categorical Observations [1] | Positive (qualifier value) |
| Value Type | Coded Entry |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 76 |
| Container Description | Gold Serum Separator tube |
| Container Volume | 5.0 |
| Container Units | mililiter |
| Specimen | Serum specimen |
| Normal Collection Volume | 2 mililiter |
| Minimum Collection Volume | 1.7 mililiter |
| Specimen Requirements | Spin down and remove serum from clot within 6 hours. |
| Specimen Handling Code | Frozen |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Hepatitis A antibodies (anti-HAV) |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Hepatitis A virus Ab [Presence] in Serum |
| Preferred Short Name or Mnemonic for Observation | anti-HAV |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Observation Identifier | Hepatitis A virus Ab [Presence] in Serum |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 77 |
| Normal Text/Codes for Categorical Observations [1] | Negative (qualifier value) |
| Abnormal Text/Codes for Categorical Observations [1] | Positive (qualifier value) |
| Value Type | Coded Entry |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 77 |
| Container Description | Gold Serum Separator tube |
| Container Volume | 5.0 |
| Container Units | mililiter |
| Specimen | Serum specimen |
| Normal Collection Volume | 2 mililiter |
| Minimum Collection Volume | 1.7 mililiter |
| Specimen Requirements | Spin down and remove serum from clot within 6 hours. |
| Specimen Handling Code | Frozen |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Hepatitis B core antibodies (anti-HBVc) |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Hepatitis B virus core Ab [Presence] in Serum |
| Preferred Short Name or Mnemonic for Observation | anti-HBVc |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Observation Identifier | Hepatitis B virus core Ab [Presence] in Serum |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 78 |
| Normal Text/Codes for Categorical Observations [1] | Negative (qualifier value) |
| Abnormal Text/Codes for Categorical Observations [1] | Positive (qualifier value) |
| Value Type | Coded Entry |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 78 |
| Container Description | Gold Serum Separator tube |
| Container Volume | 5.0 |
| Container Units | mililiter |
| Specimen | Serum specimen |
| Normal Collection Volume | 2 mililiter |
| Minimum Collection Volume | 0.8 mililiter |
| Specimen Requirements | Spin down and remove serum from clot within 6 hours. |
| Specimen Handling Code | Frozen |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Hepatitis B core antibodies (anti-HBVc) Quant |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Hepatitis B virus core Ab [Units/volume] in Serum |
| Preferred Short Name or Mnemonic for Observation | anti-HBVc Qant |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Observation Identifier | Hepatitis B virus core Ab [Units/volume] in Serum |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 79 |
| Container Description | Gold Serum Separator tube |
| Container Volume | 5.0 |
| Container Units | mililiter |
| Specimen | Serum specimen |
| Normal Collection Volume | 2 mililiter |
| Minimum Collection Volume | 1.5 mililiter |
| Specimen Requirements | Spin down and remove serum from clot within 6 hours. |
| Specimen Handling Code | Frozen |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Hepatitis B e antibodies (anti-HBVe) |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Hepatitis B virus e Ab [Presence] in Serum |
| Preferred Short Name or Mnemonic for Observation | anti-HBVe |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Observation Identifier | Hepatitis B virus e Ab [Presence] in Serum |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 80 |
| Normal Text/Codes for Categorical Observations [1] | Negative (qualifier value) |
| Abnormal Text/Codes for Categorical Observations [1] | Positive (qualifier value) |
| Value Type | Coded Entry |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 80 |
| Container Description | Gold Serum Separator tube |
| Container Volume | 5.0 |
| Container Units | mililiter |
| Specimen | Serum specimen |
| Normal Collection Volume | 2 mililiter |
| Minimum Collection Volume | 0.5 mililiter |
| Specimen Requirements | Spin down and remove serum from clot within 6 hours. |
| Specimen Handling Code | Frozen |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Hepatitis B surface antigen (HBsAg) |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Hepatitis B virus surface Ag [Presence] in Serum |
| Preferred Short Name or Mnemonic for Observation | HBsAg |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Observation Identifier | Hepatitis B virus surface Ag [Presence] in Serum |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 81 |
| Normal Text/Codes for Categorical Observations [1] | Negative (qualifier value) |
| Abnormal Text/Codes for Categorical Observations [1] | Positive (qualifier value) |
| Value Type | Coded Entry |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 81 |
| Container Description | Gold Serum Separator tube |
| Container Volume | 5.0 |
| Container Units | mililiter |
| Specimen | Serum specimen |
| Normal Collection Volume | 2 mililiter |
| Minimum Collection Volume | 0.5 mililiter |
| Specimen Requirements | Spin down and remove serum from clot within 6 hours. |
| Specimen Handling Code | Frozen |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Hepatitis B surface antibody (anti-HBVs) |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Hepatitis B virus surface Ab [Presence] in Serum |
| Preferred Short Name or Mnemonic for Observation | anti-HBVs |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Observation Identifier | Hepatitis B virus surface Ab [Presence] in Serum |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 82 |
| Normal Text/Codes for Categorical Observations [1] | Negative (qualifier value) |
| Abnormal Text/Codes for Categorical Observations [1] | Positive (qualifier value) |
| Value Type | Coded Entry |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 82 |
| Container Description | Gold Serum Separator tube |
| Container Volume | 5.0 |
| Container Units | mililiter |
| Specimen | Serum specimen |
| Normal Collection Volume | 2 mililiter |
| Minimum Collection Volume | 0.5 mililiter |
| Specimen Requirements | Spin down and remove serum from clot within 6 hours. |
| Specimen Handling Code | Frozen |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Hepatitis C antibody screen (anti-HCV) |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Hepatitis C virus Ab [Presence] in Serum |
| Preferred Short Name or Mnemonic for Observation | anti-HCV |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Observation Identifier | Hepatitis C virus Ab [Presence] in Serum |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 83 |
| Normal Text/Codes for Categorical Observations [1] | Negative (qualifier value) |
| Abnormal Text/Codes for Categorical Observations [1] | Positive (qualifier value) |
| Value Type | Coded Entry |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 83 |
| Container Description | Gold Serum Separator tube |
| Container Volume | 5.0 |
| Container Units | mililiter |
| Specimen | Serum specimen |
| Normal Collection Volume | 2 mililiter |
| Minimum Collection Volume | 0.5 mililiter |
| Specimen Requirements | Spin down and remove serum from clot within 6 hours. |
| Specimen Handling Code | Frozen |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Hepatitis C antibodies Signal to Cut-off Ratio |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Hepatitis C virus Ab Signal/Cutoff in Serum or Plasma by Immunoassay |
| Preferred Short Name or Mnemonic for Observation | anti-HCV S/CO |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Observation Identifier | Hepatitis C virus Ab Signal/Cutoff in Serum or Plasma by Immunoassay |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 84 |
| Container Description | Gold Serum Separator tube |
| Container Volume | 5.0 |
| Container Units | mililiter |
| Specimen | Serum specimen |
| Normal Collection Volume | 1.5 mililiter |
| Minimum Collection Volume | 0.8 mililiter |
| Specimen Requirements | Spin down and remove serum from clot within 6 hours. |
| Specimen Handling Code | Frozen |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Hepatitis C RNA PCR |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Hepatitis C virus RNA [Units/volume] (viral load) in Serum or Plasma by Probe and target amplification method |
| Preferred Short Name or Mnemonic for Observation | HCV PCR |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Observation Identifier | Hepatitis C virus RNA [Units/volume] (viral load) in Serum or Plasma by Probe and target amplification method |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 85 |
| Container Description | Gold Serum Separator tube |
| Container Volume | 5.0 |
| Container Units | mililiter |
| Specimen | Serum specimen |
| Normal Collection Volume | 1.5 mililiter |
| Minimum Collection Volume | 0.8 mililiter |
| Specimen Requirements | Spin down and remove serum from clot within 6 hours. |
| Specimen Handling Code | Frozen |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Penicillin |
| Element name | Data |
|---|---|
| Specimen Required | No |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Penicillin [Susceptibility] |
| Preferred Report Name for the Observation | Penicillin |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling |
| Service/Test/Observation Performance Schedule | Monday through Friday |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Penicillin [Susceptibility] |
| Expected Turn-Around Time | 3 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 86 |
| Specimen | Bacterial isolate specimen |
| Specimen Requirements | Organism must be in pure culture and actively growing. Place into large infectious container and label as " Infectious substance". |
| Specimen Handling Code | Critical ambient temperature |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Date of Last Menstrual Period |
| Element name | Data |
|---|---|
| Specimen Required | No |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Date last menstrual period |
| Preferred Report Name for the Observation | Last Menstrual Perios Date (LMP) |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Observation Identifier | Date last menstrual period |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Fasting Status |
| Element name | Data |
|---|---|
| Specimen Required | No |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Fasting status |
| Preferred Report Name for the Observation | Fasting Status |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Observation Identifier | Fasting status |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 88 |
| Normal Text/Codes for Categorical Observations [1] | Yes |
| Normal Text/Codes for Categorical Observations [2] | No |
| Value Type | Coded Entry |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Pregnancy status |
| Element name | Data |
|---|---|
| Specimen Required | No |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Pregnancy status |
| Preferred Report Name for the Observation | Is the patient pregnant? |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Observation Identifier | Pregnancy status |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 89 |
| Normal Text/Codes for Categorical Observations [1] | Yes |
| Normal Text/Codes for Categorical Observations [2] | No |
| Value Type | Coded Entry |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Urine Volume of 24 hour collection |
| Element name | Data |
|---|---|
| Specimen Required | No |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Volume of 24 hour Urine |
| Preferred Report Name for the Observation | Urine Volume 24hour collection |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Observation Identifier | Volume of 24 hour Urine |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Did the patient have a previous abnormal Pap report, treatment, or biopsy? |
| Element name | Data |
|---|---|
| Specimen Required | No |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Did the patient have a previous abnormal Pap report, treatment, or biopsy? |
| Preferred Report Name for the Observation | Did the patient have a previous abnormal Pap report, treatment, or biopsy? |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Observation Identifier | Did the patient have a previous abnormal Pap report, treatment, or biopsy? |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 91 |
| Normal Text/Codes for Categorical Observations [1] | Yes |
| Normal Text/Codes for Categorical Observations [2] | No |
| Normal Text/Codes for Categorical Observations [3] | Unknown |
| Value Type | Coded Entry |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | What is the Clinically Relevant Race? |
| Element name | Data |
|---|---|
| Specimen Required | No |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Race |
| Preferred Report Name for the Observation | Clinically Relevant Race |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Observation Identifier | Race |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 92 |
| Normal Text/Codes for Categorical Observations [1] | Asian |
| Normal Text/Codes for Categorical Observations [2] | White |
| Normal Text/Codes for Categorical Observations [3] | American Indian or Alaska Native |
| Normal Text/Codes for Categorical Observations [4] | Black or African American |
| Normal Text/Codes for Categorical Observations [5] | Native Hawaiian or Other Pacific Islander |
| Normal Text/Codes for Categorical Observations [6] | Other Race |
| Value Type | Coded Entry |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | If DOB not available, what is patient age? |
| Element name | Data |
|---|---|
| Specimen Required | No |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Age |
| Preferred Report Name for the Observation | Patient Age |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Observation Identifier | Did the patient have a previous abnormal Pap report, treatment, or biopsy? |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Dengue Virus IgG Titer Serum |
| Element name | Data |
|---|---|
| Specimen Required | No |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Dengue virus IgG Ab [Titer] in Serum |
| Preferred Report Name for the Observation | Dengue Virus IgG |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling |
| Service/Test/Observation Performance Schedule | Monday through Friday |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Dengue virus IgG Ab [Titer] in Serum |
| Expected Turn-Around Time | 2 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Dengue Virus IgM Titer Serum |
| Element name | Data |
|---|---|
| Specimen Required | No |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Dengue virus IgM Ab [Titer] in Serum |
| Preferred Report Name for the Observation | Dengue Virus IgM |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling |
| Service/Test/Observation Performance Schedule | Monday through Friday |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Dengue virus IgM Ab [Titer] in Serum |
| Expected Turn-Around Time | 2 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | WNV IgG Titer Serum |
| Element name | Data |
|---|---|
| Specimen Required | No |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | West Nile virus IgG Ab [Titer] in Serum |
| Preferred Report Name for the Observation | West Nile Virus IgG |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling |
| Service/Test/Observation Performance Schedule | Monday through Friday |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | West Nile virus IgG Ab [Titer] in Serum |
| Expected Turn-Around Time | 2 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | WNV Virus IgM Titer Serum |
| Element name | Data |
|---|---|
| Specimen Required | No |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | West Nile virus IgM Ab [Titer] in Serum |
| Preferred Report Name for the Observation | West Nile Virus IgM |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling |
| Service/Test/Observation Performance Schedule | Monday through Friday |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | West Nile virus IgM Ab [Titer] in Serum |
| Expected Turn-Around Time | 2 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | SLE IgG Titer Serum |
| Element name | Data |
|---|---|
| Specimen Required | No |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Saint Louis encephalitis virus IgG Ab [Titer] in Serum |
| Preferred Report Name for the Observation | Saint Luis Virus IgG |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling |
| Service/Test/Observation Performance Schedule | Monday through Friday |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Saint Louis encephalitis virus IgG Ab [Titer] in Serum |
| Expected Turn-Around Time | 2 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 98 |
| Container Description | Gold Serum Separator tube |
| Container Description | Red, No Additive tube |
| Container Volume | 5.0 |
| Container Volume | 5.0 |
| Container Units | mililiter |
| Container Units | mililiter |
| Specimen | Serum specimen |
| Normal Collection Volume | 1 milliliter |
| Minimum Collection Volume | 0.5 milliliter |
| Specimen Requirements | Protect from light. Allow serum tube to clot completely at room temperature. Separate serum or plasma from cells ASAP or within 30 minutes of collection. |
| Specimen Handling Code | Refrigerated temperature |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | SLE IgM Titer Serum |
| Element name | Data |
|---|---|
| Specimen Required | No |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Saint Louis encephalitis virus IgM Ab [Titer] in Serum |
| Preferred Report Name for the Observation | Saint Luis Virus IgM |
| Orderability | Yes |
| Nature of Service/Test/Observation | A |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling |
| Service/Test/Observation Performance Schedule | Monday through Friday |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Saint Louis encephalitis virus IgM Ab [Titer] in Serum |
| Expected Turn-Around Time | 2 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 99 |
| Container Description | Gold Serum Separator tube |
| Container Description | Red, No Additive tube |
| Container Volume | 5.0 |
| Container Volume | 5.0 |
| Container Units | mililiter |
| Container Units | mililiter |
| Specimen | Serum specimen |
| Normal Collection Volume | 1 milliliter |
| Minimum Collection Volume | 0.5 milliliter |
| Specimen Requirements | Protect from light. Allow serum tube to clot completely at room temperature. Separate serum or plasma from cells ASAP or within 30 minutes of collection. |
| Specimen Handling Code | Refrigerated temperature |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Creatinine Clearance in 24 hours |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Creatinine renal clearance in 24 hour |
| Preferred Report Name for the Observation | Creatinine Clearance in 24 hours |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Observations Required to Interpret the Observation | Race |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling |
| Service/Test/Observation Performance Schedule | Monday through Friday |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Creatinine renal clearance in 24 hour |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Creatinine in 24 hr Urine |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Creatinine [Mass/volume] in 24 hour Urine |
| Preferred Report Name for the Observation | Creatinine in 24 hr Urine |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling |
| Service/Test/Observation Performance Schedule | Monday through Friday |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Creatinine [Mass/volume] in 24 hour Urine |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 101 |
| Container Description | Sterile, plastic, leak proof container |
| Container Volume | 2000 |
| Container Units | milliliter |
| Specimen | Urine specimen |
| Normal Collection Volume | 20 milliliter |
| Minimum Collection Volume | 4 milliliter |
| Specimen Requirements | Keep refrigerated |
| Specimen Handling Code | Refrigerated temperature |
| Specimen Preference | Preferred |
| Element name | Data |
|---|---|
| Record-Level Event Code | Add record to master file |
| Effective Date/Time | 2013-12-19 2:53:10pm |
| Primary Key Value - MFE | Protein in 24 hour Urine |
| Element name | Data |
|---|---|
| Specimen Required | Yes |
| Producer ID | Century Hospital Clinical Laboratory |
| Other Service/Test/Observation IDs for the Observation | Protein [Mass/volume] in 24 hour Urine |
| Preferred Report Name for the Observation | 24 hour Urine Protein |
| Orderability | No |
| Nature of Service/Test/Observation | A |
| Factors that may Affect the Observation | Insufficient specimen, Improper labeling |
| Service/Test/Observation Performance Schedule | Monday through Friday |
| Exclusive Test | This test can be included with any number of other tests |
| Diagnostic Service Sector ID | Laboratory |
| Observation Identifier | Protein [Mass/volume] in 24 hour Urine |
| Expected Turn-Around Time | 1 day |
| Element name | Data |
|---|---|
| Sequence Number - Test/Observation Master File | 102 |
| Container Description | Sterile, plastic, leak proof container |
| Container Volume | 2000 |
| Container Units | milliliter |
| Specimen | Urine specimen |
| Normal Collection Volume | 20 milliliter |
| Minimum Collection Volume | 4 milliliter |
| Specimen Requirements | Keep refrigerated |
| Specimen Handling Code | Refrigerated temperature |
| Specimen Preference | Preferred |